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DiMauro

Showing results (231-240 of 1,071) with videos related to

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Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegiaL P Rowland, M Hirano, S DiMauro, et al.
Advances in Neurology|October 9, 1999
Mitochondrial genes for generalized epilepsiesS DiMauro, R Kulikova, K Tanji, et al.
Journal of Child Neurology|June 27, 2000
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuriaC Bruno, M Bado, C Minetti, et al.
Brain Pathology (Zurich, Switzerland)|October 1, 1993
Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical studyM Sparaco, A Hirano, M Hirano, et al.
American Journal of Human Genetics|March 1, 1993
The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Journal of Anxiety Disorders|September 28, 2014
A historical review of trauma-related diagnoses to reconsider the heterogeneity of PTSDJennifer DiMauro, Sarah Carter, Johanna B Folk, et al.
Neurology|May 1, 1989
Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutationA F Miranda, S Ishii, S DiMauro, et al.
Trends in Molecular Medicine|June 18, 2010
Therapeutic prospects for mitochondrial diseaseEric A Schon, Salvatore DiMauro, Michio Hirano, et al.
Archives of Neurology|April 1, 1985
Immunocytochemical analysis of normal and acid maltase-deficient muscle culturesA F Miranda, S Shanske, A P Hays, et al.
Neurology|September 1, 1973
Thyrotoxic periodic paralysis. Function of sarcoplasmic reticulum and muscle glycogenA Takagi, D L Schotland, S DiMauro, et al.
Pageof 108

Showing results (231-240 of 1,071) with videos related to

Sort By:
Pageof 108
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegiaL P Rowland, M Hirano, S DiMauro, et al.
Advances in Neurology|October 9, 1999
Mitochondrial genes for generalized epilepsiesS DiMauro, R Kulikova, K Tanji, et al.
Journal of Child Neurology|June 27, 2000
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuriaC Bruno, M Bado, C Minetti, et al.
Brain Pathology (Zurich, Switzerland)|October 1, 1993
Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical studyM Sparaco, A Hirano, M Hirano, et al.
American Journal of Human Genetics|March 1, 1993
The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Journal of Anxiety Disorders|September 28, 2014
A historical review of trauma-related diagnoses to reconsider the heterogeneity of PTSDJennifer DiMauro, Sarah Carter, Johanna B Folk, et al.
Neurology|May 1, 1989
Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutationA F Miranda, S Ishii, S DiMauro, et al.
Trends in Molecular Medicine|June 18, 2010
Therapeutic prospects for mitochondrial diseaseEric A Schon, Salvatore DiMauro, Michio Hirano, et al.
Archives of Neurology|April 1, 1985
Immunocytochemical analysis of normal and acid maltase-deficient muscle culturesA F Miranda, S Shanske, A P Hays, et al.
Neurology|September 1, 1973
Thyrotoxic periodic paralysis. Function of sarcoplasmic reticulum and muscle glycogenA Takagi, D L Schotland, S DiMauro, et al.
Pageof 108